Showing 1 - 20 results of 24 for search 'T. van Heyningen', query time: 0.04s
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Cape lives of the eighteenth century by Elizabeth van Heyningen
Published 2013-07-01
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Genetic control of mitochondrial enzymes in human-mouse somatic cell hybrids. by Van Heyningen, V, Craig, I, Bodmer, W
Published 1973Journal article -
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The development of an ultra-short, maternal mental health screening tool in South Africa by T. van Heyningen, L. Myer, M. Tomlinson, S. Field, S. Honikman
Published 2019-01-01
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Hsp90 selectively modulates phenotype in vertebrate development. by Patricia L Yeyati, Ruth M Bancewicz, John Maule, Veronica van Heyningen
Published 2007-03-01
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Molecular genetic mapping of the multiple endocrine neoplasia type 1 locus. by Pang, J, Pook, M, Eubanks, J, Jones, C, van Heyningen, V, Evans, G, Thakker, R
Published 1992Journal article -
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The beta2-microglobulin gene is on chromosome 15 and not in the HL-A region. by Goodfellow, P, Jones, E, Van Heyningen, V, Solomon, E, Bobrow, M, Miggiano, V, Bodmer, W
Published 1975Journal article -
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Linkage relationships of the HL-A system and beta 2 microglobulin. by Goodfellow, P, Jones, E, van Heyningen, V, Solomon, E, Kennett, R, Bobrow, M, Bodmer, W
Published 1975Journal article -
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Linkage relationships of the HL-A system and beta2 microglobulin. by Goodfellow, P, Jones, E, van Heyningen, V, Solomon, E, Kennett, R, Bobrow, M, Bodmer, W
Published 1975Journal article -
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EagI and NotI linking clones from human chromosomes 11 and Xp. by Pook, M, Thakrar, R, Pottinger, B, Harding, B, Porteous, D, van Heyningen, V, Cowell, J, Jones, C, Povey, S, Davies, K, Thakker, R
Published 1996Journal article -
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Functional assessment of disease-associated regulatory variants in vivo using a versatile dual colour transgenesis strategy in zebrafish. by Shipra Bhatia, Christopher T Gordon, Robert G Foster, Lucie Melin, Véronique Abadie, Geneviève Baujat, Marie-Paule Vazquez, Jeanne Amiel, Stanislas Lyonnet, Veronica van Heyningen, Dirk A Kleinjan
Published 2015-06-01
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Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects. by Williamson, K, Rainger, J, Floyd, J, Ansari, M, Meynert, A, Aldridge, K, Rainger, J, Anderson, C, Moore, A, Hurles, M, Clarke, A, van Heyningen, V, Verloes, A, Taylor, MS, Wilkie, A, Fitzpatrick, DR
Published 2014Journal article